EP2815763B1 - Therapeutic agent for inflammatory disease - Google Patents

Therapeutic agent for inflammatory disease Download PDF

Info

Publication number
EP2815763B1
EP2815763B1 EP13751092.1A EP13751092A EP2815763B1 EP 2815763 B1 EP2815763 B1 EP 2815763B1 EP 13751092 A EP13751092 A EP 13751092A EP 2815763 B1 EP2815763 B1 EP 2815763B1
Authority
EP
European Patent Office
Prior art keywords
seq
amino acid
monoclonal antibody
acid sequence
therapeutic agent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Not-in-force
Application number
EP13751092.1A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP2815763A4 (en
EP2815763A1 (en
Inventor
Shuji Sato
Takeshi Goto
Naoya Ohmori
Kueichen Chiang
Yayoi Shimada
Masafumi Inomata
Toru Kusano
Takahiro Hiratsuka
Takayuki Noguchi
Satoshi Hagiwara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Josai University Corp
JOSAI UNIV CORP
Original Assignee
Josai University Corp
JOSAI UNIV CORP
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Josai University Corp, JOSAI UNIV CORP filed Critical Josai University Corp
Publication of EP2815763A1 publication Critical patent/EP2815763A1/en
Publication of EP2815763A4 publication Critical patent/EP2815763A4/en
Application granted granted Critical
Publication of EP2815763B1 publication Critical patent/EP2815763B1/en
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/44—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material not provided for elsewhere, e.g. haptens, metals, DNA, RNA, amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
    • C07K2317/14—Specific host cells or culture conditions, e.g. components, pH or temperature
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/55—Fab or Fab'
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565—Complementarity determining region [CDR]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622—Single chain antibody (scFv)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding

Definitions

  • the present invention relates to a novel therapeutic agent for inflammatory disease comprising as an effective ingredient a monoclonal antibody or an antigen binding fragment thereof.
  • DAMPs Damage-associated molecular pattern molecules
  • sepsis is a severe systemic infectious disease in which bacteria continuously or intermittently enter the blood from an infection focus, which is caused by diseases such as infectious diseases, cirrhosis, renal failure, diabetes and dystocia, or by therapies against injury or disease, such as indwelling catheter, transfusion device, dialysis or tracheostomy.
  • diseases such as infectious diseases, cirrhosis, renal failure, diabetes and dystocia
  • therapies against injury or disease such as indwelling catheter, transfusion device, dialysis or tracheostomy.
  • sepsis is not restricted to the invasion by a microorganism into a host, but is defined to include clinical conditions of infectious diseases, in which two or more of the following are met: (1) body temperature >38°C or ⁇ 36°C; (2) heart rate >90 beats/min.; (3) frequency of respiration >20 breaths/min.
  • Non-patent Literature 1 Crit. Care Med., 20:864-874, 1992
  • Sepsis further includes organ dysfunction, severe sepsis complicated with hypoperfusion or hypotension, lactic acidosis, hypouresis and septic shock complicated with consciousness disorder
  • Non-patent Literature 2 Chest,101:1644-1655,1992 ). Severe sepsis and septic shock induce disseminated intravascular coagulation syndrome (DIC), adult respiratory distress syndrome (ARDS) and multiple organ dysfunction (MODS).
  • DIC intravascular coagulation syndrome
  • ARDS adult respiratory distress syndrome
  • MODS multiple organ dysfunction
  • the causative bacteria of sepsis are mainly staphylococci, streptococci, Escherichia coli, Pseudomonas aeruginosa, Klebsiella and Enterobacter. By the infection of these bacteria, high fever, chill, tachycardia and strong systemic symptoms are exhibited, and existence of the infective bacteria is often confirmed in the arterial blood, venous blood, spinal fluid and bone marrow fluid.
  • a method for prevention or therapy of sepsis now employed is carried out by administering the best antibiotic against the causative bacterium after detecting the causative bacterium and determining the sensitivities thereof to antibiotics, and by simultaneously promoting the defending ability of the host by fluid replacement, replenishment of electrolytes, improvement of hypoproteinemia, replenishment of nutrients, administration of ⁇ -globulin and the like.
  • treatments such as removal of lesion by surgery, improvement of circulatory dysfunction, administration of opsonin-activating substances, administration of adenocorticotropic hormones, administration of synthetic protease inhibitors, and the like are carried out.
  • the death rate of sepsis varies from 10%-20% to 50% depending on the report. Forty percent of sepsis cases are complicated with septic shock, and the prognosis of the shock is bad. There is a report which shows the death rate of the shock is 77 to 90%. Therefore, the primary object of the therapy is the prevention of the septic shock. If the changes which occurs in the initial stage of the shock are grasped and early diagnosis is attained, early treatment can be attained and improvement of prognosis is expected. However, although a number of anti-shock drugs and therapeutic methods have been studied, almost none of them were judged effective.
  • cytokines such as tumor necrosis factor (TNF), interleukin 1 (IL-1), interleukin 6 (IL-6) and interleukin 8 (IL-8), which are excessively produced by monocytes, macrophages, vascular endothelial cells and the like in response to the infectious stimuli (such as bacterial cells per se, endotoxins, cell wall components which are peptide glycan/teichoic acid complexes and exotoxins).
  • TNF tumor necrosis factor
  • IL-1 interleukin 1
  • IL-6 interleukin 6
  • IL-8 interleukin 8
  • complement system coagulation system
  • kinin system adrenocorticotropic hormone/endorphin system
  • adrenocorticotropic hormone/endorphin system are also activated, and the systemic inflammatory reaction of which underlying symptom is vascular endothelial disorder is induced.
  • elastase originated from granulocytes and active oxygen has been shown.
  • Non-patent Literature 3 Lancet,351:929-933,1998 , JAMA,271:1836-1843,1994 ).
  • Non-patent Literature 4 Nath. J. Med.,55:132-141,1999 .
  • extracellular histones released in response to inflammatory challenge might be mediators, which contribute to endothelial dysfunction, organ failure and death during sepsis.
  • the authors concluded that they can be targeted pharmacologically by inhibitors, for instance anti-histone blocking antibodies, as well as used as biomarkers for prognosis of sepsis and other diseases.
  • inhibitors for instance anti-histone blocking antibodies
  • Non-patent Literature 5 Extracellular histones are major mediators of death in sepsis; Nat Med. 2009 November ; 15(11): 1318-1321 ).
  • EP 1 820 855 A1 relates to anti-histone H1 antibodies, hybridomas for the production thereof, and polypeptides, which are useful for suppressing, predicting, or diagnosing transplant rejection in organ transplantation.
  • EP 1 820 855 A1 discloses the hybridoma 16G9 producing an anti-histone H1 antibody that was also used in the context of noninvasively administering vaccine through the skin in EP 2 196 212 A1 .
  • the present inventors have found that a monoclonal antibody or an antigen binding fragment thereof which can specifically recognize a peptide consisting of an amino acid sequence represented by SSVLYGGPPSAA (SEQ ID NO:1) has excellent advantageous effects on inflammatory diseases in which histone is involved.
  • the present invention is based on these findings.
  • an object of the present invention is to provide a novel therapeutic agent for inflammatory diseases.
  • the present invention provides a therapeutic agent for use in a treatment of an inflammatory disease as defined in claim 1.
  • the therapeutic agent comprises a monoclonal antibody or an antigen binding fragment thereof which binds to a peptide consisting of an amino acid sequence represented by SSVLYGGPPSAA (SEQ ID NO:1) or a conjugate of the peptide and a pharmaceutically acceptable carrier.
  • SSVLYGGPPSAA SEQ ID NO:1
  • Preferred embodiments are set forth in subclaims.
  • the hybridoma of the present invention Mouse-Mouse hybridoma SSV-C 93-3 was deposited at National Institute of Technology and Evaluation, Patent Microorganisms Depositary (Address: Biotechnology Headquarter, 2-5-8 Kazusa Kamatari, Kisarazu-shi, Chiba-ken, Japan) on the original deposition day of August 17, 2010 under the deposition number NITE BP-972.
  • the monoclonal antibody of the present invention or an antigen binding fragment thereof binds to a peptide consisting of an amino acid sequence represented by SSVLYGGPPSAA (SEQ ID NO:1) or a conjugate of the peptide and a pharmaceutically acceptable carrier.
  • SSVLYGGPPSAA SEQ ID NO:1
  • the present inventors have found that such a monoclonal antibody or an antigen binding fragment thereof has an excellent therapeutic effect on inflammatory diseases.
  • Inflammatory diseases in the present invention are preferably inflammatory diseases in which histone is involved, more preferably acute inflammatory diseases, more preferably sepsis, renal ischemia reperfusion injury or renal failure, still more preferably sepsis, renal ischemia reperfusion injury or acute renal failure, still further preferably sepsis.
  • the above-mentioned antibody or an antigen binding fragment thereof is against a peptide consisting of an amino acid sequence represented by SSVLYGGPPSAA (SEQ ID NO:1) or, the peptide and a pharmaceutically acceptable carrier.
  • the above-mentioned antibody or an antigen binding fragment thereof specifically binds to histone H1, histone H3 and histone H4.
  • An antibody or an antigen binding fragment thereof which has such binding capacity may be especially advantageously used in the treatment of inflammatory diseases as shown in 8-2 in Example hereinbelow described.
  • the above-mentioned antibody or an antigen binding fragment thereof has a higher binding affinity for core histone than for linker histone (histone H1).
  • core histone is histone H2A, H2B, H3 or H4, and more preferably H2A, H3 or H4.
  • the antibody of the present invention or an antibody binding fragment thereof also comprises a heavy chain and/or a light chain.
  • Each of a light chain and a heavy chain has a variable region at its N-terminal, and each variable region contains four framework regions (FR) and three complementarity determining regions (CDR) in an alternate fashion.
  • FR framework regions
  • CDR complementarity determining regions
  • residues in a variable region are numbered according to the system devised by Kabat et al. The system is described in Kabat et al., 1987, Sequences of Proteins of Immunological Interest, US Department of Health and Human Services, NIH, USA . Unless otherwise stated, this numbering system is used in the present specification. Numbering based on the method by Kabat et al. can be easily performed, for example, using the web site at http://www.bioinf.org.uk/abysis/tools/analyze.cgi.
  • the Kabat nomenclature of residues does not necessarily correspond to the linear numbering of amino acid residues directly.
  • An actual linear amino acid sequence in either a structural element of the basic structure of a variable region, a framework or a CDR may have a fewer or additional amino acid compared with the strict Kabat numbering depending on its truncation or insertion.
  • correct Kabat numbering of residues will be determined by aligning homologous residues in a sequence numbered according to the "standard" Kabat numbering and in a sequence of the antibody.
  • the light chain variable region of the antibody of the present invention or an antigen binding fragment thereof comprises CDR1 consisting of an amino acid sequence represented by RASSSVSYMH (SEQ ID NO:2), CDR2 consisting of an amino acid sequence represented by ATSNLAS (SEQ ID NO:3) and CDR3 consisting of an amino acid sequence represented by QQWSSNPWT (SEQ ID NO:4).
  • the above-mentioned light chain variable region comprises an amino acid sequence represented by Position 23 to Position 128 of SEQ ID NO:6.
  • the heavy chain variable region of the antibody of the present invention or an antigen binding fragment thereof comprises CDR1 consisting of an amino acid sequence represented by GYNMN (SEQ ID NO:7), CDR2 consisting of an amino acid sequence represented by NINPYYGSTSYNQKFKG (SEQ ID NO:8) and CDR3 consisting of an amino acid sequence represented by SPYYSNYWRYFDY (SEQ ID NO:9).
  • the above-mentioned heavy chain variable region comprises an amino acid sequence represented by Position 20 to Position 141 of SEQ ID NO:11.
  • the antibody of the present invention or an antigen binding fragment thereof comprises a light chain variable region comprising CDR1 consisting of an amino acid sequence represented by RASSSVSYMH (SEQ ID NO:2), CDR2 consisting of an amino acid sequence represented by ATSNLAS (SEQ ID NO:3) and CDR3 consisting of an amino acid sequence represented by QQWSSNPWT (SEQ ID NO:4), and a heavy chain variable region comprising a heavy chain variable region comprising CDR1 consisting of an amino acid sequence represented by GYNMN (SEQ ID NO:7), CDR2 consisting of an amino acid sequence represented by NINPYYGSTSYNQKFKG (SEQ ID NO:8) and CDR3 consisting of an amino acid sequence represented by SPYYSNYWRYFDY (SEQ ID NO:9).
  • the antibody of the present invention or antigen binding fragment thereof comprises a light chain variable region comprising an amino acid sequence represented by Position 23 to Position 128 of SEQ ID NO:6 and a heavy chain variable region comprising an amino acid sequence represented by Position 20 to Position 141 of SEQ ID NO:11.
  • the above-mentioned monoclonal antibody or an antigen binding fragment thereof can down-regulate the activity of ATP synthase.
  • the above-mentioned ATP synthase is mitochondria ATP synthase.
  • the monoclonal antibody of the present invention is preferably a chimeric antibody.
  • chimeric antibody Those skilled in the art can produce these antibodies according to known technologies in the art as described in, for example, Morrison, S.L., Oi, V. T., "immunoglobulin genes” Academic Press (London), 260-274 (1989 ); Roguska, M. L. et. Al., Humanization of murine monoclonal antibodies through variable domain resurfacing, Proc. Natl. Acad. Sci. USA, 91, 969-973 (1994 ); Tomizuka, K. et. al.
  • the above-mentioned antigen binding fragment is preferably Fab, Fab', (Fab') 2 , Fv or scFv.
  • the above-mentioned monoclonal antibody or an antigen binding fragment thereof is produced by a hybridoma Mouse-Mouse hybridoma SSV-C93-3.
  • the monoclonal antibody of the present invention or an antigen binding fragment thereof, and a hybridoma can be produced, for example, as follows. That is, first, the hybridoma of the present invention can be obtained using a peptide comprising an amino acid sequence represented by SSVLYGGPPSAA (SEQ ID NO:1) or a conjugate of this peptide and a pharmaceutically acceptable carrier as an antigen by fusing mammalian plasma cells (immune cells) immunized by this sensitizing antigen with mammalian myeloma cells, and cloning and screening the resulting hybridomas. Then the monoclonal antibody of the present invention can be obtained by culturing the hybridoma of the present invention and collecting antibody produced by it.
  • SSVLYGGPPSAA SEQ ID NO:1
  • a pharmaceutically acceptable carrier as an antigen by fusing mammalian plasma cells (immune cells) immunized by this sensitizing antigen with mammalian myelo
  • any common administration methods in the art can be used.
  • they include intraperitoneal injection, intrasplenic injection, intramuscular injection, subcutaneous injection, intradermal injection, oral administration, transmucosal administration, transdermal administration, but preferably they are intraperitoneal injection, intrasplenic injection.
  • the dosage interval of a sensitizing antigen is appropriately determined depending on a dose of the sensitizing antigen, a species of the mammal and the like. For example, it can be several times per month.
  • Mammals to be immunized are not particularly limited, but preferably selected after considering, for example, compatibility with myeloma cells used for cell fusion. They include, for example, mouse, rat and hamster. Preferably, the mammal is mouse.
  • splenic cells are preferably used as immune cells.
  • Myeloma cells used for the present invention include, for example, P3 (P3X63Ag8.653) ( J. Immunol., 123,1548, 1978 ), p3-U1 ( Current Topics in Micro-biology and Immunology, 81, 1-7,1978 ), NS-1 ( Eur. J. Immunol., 6, 511-519, 1976 ), MPC-11 ( Cell, 8, 405-415, 1976 ), Sp2/0-Ag14 ( Nature, 276, 269-270, 1978 ), FO ( J. Immunol. Meth., 35, 1-21, 1980 ), S194 ( J. Exp. Med., 148, 313-323, 1978 ) and R210 ( Nature, 277, 131-133, 1979 ).
  • the myeloma cell is preferably P3 or p3-U1, more preferably P3.
  • Immune cells and myeloma cells can be fused, for example, by a method according to Milstein et. al. (Methods Enzymol., 73, 3-46, 1981 ). Specifically, cell fusion can be performed, for example, by mixing immune cells and myeloma cells in culture medium in the presence of a fusion promoter. Then, addition of culture medium and centrifugation can be appropriately repeated during cell fusion to produce hybridomas.
  • Culture media used for cell fusion include, for example, culture media usually used in cell fusion such as RPMI-1640 culture medium and MEM culture medium. Further, blood serum supplements such as fetal calf serum (FBS) can be suitably used together.
  • FBS fetal calf serum
  • Temperature for cell fusion is preferably 25 to 37°C, and more preferably 30 to 37°C.
  • a mixing ratio of myeloma cells and immune cells is preferably about 1:1 to 1:10.
  • Fusion promoters may include, for example, polyethylene glycol (PEG) and Sendai Virus (HVJ).
  • PEG polyethylene glycol
  • HVJ Sendai Virus
  • the fusion promoter is preferably PEG.
  • the molecular weight of PEG can be suitably selected, and for example, the average molecular weight can be between about 1,000 and 6,000.
  • the concentration of PEG in culture medium is preferably about 30 to 60% (W/V).
  • Auxiliary agents such as dimethyl sulfoxide can be suitably added to culture medium as desired.
  • Selection of the hybridoma of the present invention can be performed by culturing hybridomas obtained by cell fusion, for example, in common selection medium such as HAT culture medium, and using the limiting dilution method to conduct screening for, for example, on the basis of an indicator such as an antibody titer against a peptide consisting of an amino acid sequence represented by SSVLYGGPPSAA (SEQ ID NO:1) or a conjugate of the peptide and a pharmaceutically acceptable carrier.
  • a culture period in HAT culture medium is a sufficient period for cells (non-fused cells) other than the hybridoma of interest to die, and usually can be several days to several weeks.
  • the hybridoma of the present invention obtained in this way can be subcultured in common culture medium, and also can be stored for a long time in liquid nitrogen.
  • Methods of harvesting the monoclonal antibody of the present invention or an antibody binding fragment thereof include, for example, a method where hybridoma is cultured according to the conventional method to obtain monoclonal antibody and the like from the culture supernatant or a method where hybridoma is administered to a compatible mammal for proliferation and monoclonal antibody and the like is obtained from its ascitic fluid.
  • the former method is preferred for obtaining highly pure antibody while the latter method is preferred for producing a large amount of antibody.
  • the monoclonal antibody of the present invention or an antibody binding fragment thereof can be purified to a high purity by methods such as salting-out, gel filtration and affinity chromatography.
  • inflammatory diseases are preferably inflammatory diseases in which histone is involved, more preferably acute inflammatory diseases, more preferably sepsis, renal ischemia reperfusion injury or renal failure, still more preferably sepsis, renal ischemia reperfusion injury or acute renal failure, still further preferably sepsis.
  • the monoclonal antibody of the present invention or an antigen binding fragment thereof may be used as it is, or may be used as a pharmaceutical composition along with a pharmacologically acceptable additive. Therefore, according to one aspect of the present invention, provided is a pharmaceutical preparations for treating inflammatory diseases comprising the monoclonal antibody of the present invention or an antigen binding fragment thereof.
  • the therapeutic agent for treating sepsis of the present invention can be prepared, for example, by solving the monoclonal antibody of the present invention in injectable saline, injectable distilled water, an injectable buffer solution and the like.
  • the composition for immunosuppression of the present invention may further contain a suitable solvent, a solubilizing agent, a preserving agent, a stabilizing agent, an emulsifying agent, a suspending agent, a soothing agent, a tonicity adjusting agent, a buffer, an excipient, a thickener, a coloring agent, a known carrier (various liposomes, polyamino acid carriers, synthetic macromolecules, naturally-occurring polymers and the like) and the like.
  • a method of treating inflammatory disease comprising administrating an effective amount of the monoclonal antibody of the present invention or an antigen binding fragment thereof.
  • the term "treating" means alleviating established pathology.
  • a method of reducing risk of a subject for developing inflammatory disease comprising administering an effective amount of the monoclonal antibody of the present invention or an antigen binding fragment thereof to the subject.
  • inflammatory diseases are preferably inflammatory diseases in which histone is involved, more preferably acute inflammatory diseases, more preferably sepsis, renal ischemia reperfusion injury or renal failure, still more preferably sepsis, renal ischemia reperfusion injury or acute renal failure, still further preferably sepsis.
  • the monoclonal antibody of the present invention or an antigen binding fragment thereof can exert a prominent immunosuppressive effect. It is surprising that the above-mentioned monoclonal antibody or an antigen binding fragment thereof which may be used in the treatment of inflammatory diseases can exert an immunosuppressive effect. Therefore, according to one aspect, the monoclonal antibody of the present invention or an antigen binding fragment thereof is used as an immunosuppressive agent.
  • the above-mentioned subjects are preferably a mammal, more preferably a human.
  • the monoclonal antibody of the present invention or an antigen binding fragment thereof may be simultaneously or sequentially administered to a mammal in combination with other agents used for inflammatory diseases.
  • the monoclonal antibody of the present invention or an antigen binding fragment thereof can be administered systemically or locally.
  • Specific methods of administration include infusion, intravenous injection, intramuscular injection, subcutaneous injection, intradermal injection, oral administration, transmucosal administration and transdermal administration.
  • the effective amount of the monoclonal antibody of the present invention or an antigen binding fragment is not particularly limited, and can be suitably determined by the person skilled in the art depending on species, nature, sex, age, symptoms and the like of the subject.
  • effective amounts include one or several doses of 0.05 to 40 mg/kg weight/day, preferably 2 to 10 mg/kg weight/day.
  • a conjugate of a peptide consisting of an amino acid sequence represented by SEQ ID NO:1 and KLH were used.
  • a peptide consisting of an amino acid sequence represented by SEQ ID NO:1 was synthesized by the Fmoc peptide solid phase synthesis method (a manufacturing instrument; Applied Biosystems ABI 430).
  • a conjugate of the above-mentioned peptide and KLH (SIGMA) was synthesized by stirring 5 mg of the above-mentioned peptide, about 20 mg KLH and 30 ⁇ g glutaraldehyde (Katayama Chemical Industries Co., Ltd.) in phosphate buffer (pH 8.0) at room temperature for about 6 hours.
  • Suspension (the concentration of the antigen: 0.25 mg/mL) was obtained by mixing 0.8 mL of a solution in which the antigenic substance was dissolved in PBS (the concentration of the antigenic substance: 0.5 mg/mL) and 0.8 mL complete Freund's adjuvant (Wako Pure Chemical Industries, Ltd.). Then, 0.2 mL of this suspension was intraperitoneally administered to a BALB/c mouse. This suspension in the same amount was further administered to the mouse every two weeks. Then, 16 weeks after the administration was started, 0.2 mL of a solution in which the antigen was dissolved in PBS (the concentration of the antigen: 600 to 1000 mg/mL) was intraperitoneally administered to the mouse as a final dose.
  • FCS JRH BIOSCIENCES
  • IMDM IMDM
  • HAT culture medium was replaced every 2 to 3 days, and after 10 days, it was switched to HT culture medium (HT powder (HT MEDIA SUPPLEMENT, SIGMA) was dissolved in 10 mL serum free IMDM culture medium, which was then diluted 50 times with 10% FCS containing IMDM culture medium.), and cultured in an incubator at 37°C/5% CO 2 for three days. After that, the culture medium (HT culture medium) was replaced every 2 to 3 days. After verifying cell growth under a microscope, the culture supernatants (about 100 mL) were collected. Using the culture supernatants, screening of hybridoma was performed by measuring antibody titers.
  • a buffer solution containing the above-mentioned antigenic substance (5 mg) (Baicarbonate buffer: 100 mM NaHCO 3 -NaOH, pH 9.2 to 9.5, the concentration of the peptide: 1 ⁇ g/mL) was added to a 96 well flat bottom plate in an amount of 50 ⁇ L per well, and allowed to stand for coating at room temperature for 2 hours.
  • the plate was washed 3 times with wash buffer (PBST), and then blocking buffer (3% skim milk 1% BSA, PBS) was added in an amount of 200 to 250 ⁇ L/well to react at 4°C for one full day, and then washed 3 times.
  • PBST wash buffer
  • blocking buffer 3% skim milk 1% BSA, PBS
  • the culture supernatant of hybridoma was added in an amount of 100 ⁇ L/well, which was allowed to react at 37°C for 4 hours or at 4°C for one full day.
  • biotin-labeled anti-mouse IgG SIGMA diluted 10000 times with dilution buffer (10 mM Tris-HCl (pH 8.0), 0.9% (W/V) NaCl, 0.05% (W/V) Tween 20) was added in an amount of 50 ⁇ L/well, which was allowed to react at room temperature for 2 hours.
  • alkaline phosphatase labeled Streptaridin diluted 1000 times with dilution buffer was added in an amount of 50 ⁇ L/well, which was allowed to react at room temperature for 1 to 2 hours. Then washing was performed 6 times, and fluorescent substrate buffer (Attophos substrate buffer, Roche Diagnostics K.K.) was added in an amount of 50 ⁇ L/well, and the plate was shaded to allow fluorescence to develop. Fluorescence intensity was measured in CytoFluorII (PerSeptive Biosystems).
  • Limiting dilution was further performed so that the selected hybridoma was diluted to 0.5 to 1 cell/well with 15% FCS 10% HCF containing IMDM culture medium. After culturing in an incubator at 37°C/5% CO 2 for about three to four days, antibody titers were measured as described above to select hybridomas showing a high antibody yield. Limiting dilution was further repeated to obtain hybridomas which produce monoclonal antibody against the above-mentioned antigenic substance. Among these, the hybridoma with the highest antibody titer was selected and designated as Mouse-Mouse hybridoma SSV-C 93-3.
  • Hybridoma Mouse-Mouse hybridoma SSV-C 93-3 was cultured using 15% FCS containing RPMI culture medium (1x10 6 cells/mL). Then, hybridoma culture medium was collected, and filtered through a filter in order to remove dead cell debris. Then, ammonium sulfate was added to the culture supernatant to a final concentration of 40%, and stirred at 40°C for 1 hour. Then, centrifugation (3000 g, 30 minutes, 4°C) was performed, and the supernatant was discarded to collect precipitate. The precipitate was dissolved in a volume of PBS equivalent to a 1/10 amount of the above-mentioned culture supernatant, and dialyzed against PBS overnight.
  • the above-mentioned precipitate was diluted twice with 20 mM sodium phosphate buffer (pH 7.0), and loaded onto a HiTrap NHS activated column along with 1 M Tris-HCl buffer. Then, antibody was eluted with a 0.1 M glycine HCl solution (pH 2.7), and collected in fraction tubes.
  • the isotype of the monoclonal antibody (SSVmAb) of Example 1 was determined to be IgG1.
  • Test Example 2 Determination of the affinity of SSVmAb for core histone
  • WO2006/025580 has reported the monoclonal antibody (16G9mAb) produced by hybridoma 16G9 (Deposition Number FERM BP-10413) as an anti H1 monoclonal antibody which can be used for immunosuppression and which binds to a peptide consisting of an amino acid sequence represented by SEQ ID NO:1.
  • histone H1 which is an antigen of Reference Example 1 (16G9mAb)
  • core histone H2A, H2B, H3 and H4 which are histone H1 antigen analogs
  • a 96 well microplate was coated with histone H1, H2A, H2B, H3 or H4. Each histone used was dissolved in 100 mM sodium carbonate buffer (pH 9.3). The plate was washed with PBS-tween 20 (0.05%), and blocked with 3% skim milk and 1% BSA for 1 hour. To each well, 5 ⁇ g/mL SSVmAb was added, and incubated for 1 hour. Bound SSVmAb was detected using peroxidase (HRP) conjugated anti mouse IgG1 Ab (SIGMA), and incubated for 1 hour.
  • HRP peroxidase
  • SIGMA peroxidase conjugated anti mouse IgG1 Ab
  • Bound SSVmAb was detected using the ABTS [2,2'-azino-bis(3-ethylbenzothiazoline-sulfonic acid)] substrate solution, and absorbance at 405 nm was measured using Multiskan Ascent (Thermo Fisher Scientific Inc., Waltham, MA).
  • the affinities for histone H2A, H2B, H3 or H4 were higher than the affinity for histone H1.
  • Spleen lymphocytes from a naive DA rat (responsive cells) and spleen lymphocytes from a LEW rat treated with mitomycin-C (Kyowa Hakko Kogyo Co., Ltd.) (stimulated cells) were used.
  • the responsive cells were adjusted to 5x10 5 cells/mL with 10% FCS-RPMI culture medium, and the stimulated cells were adjusted to 8x10 6 cells/mL with 10% FCS-RPMI culture medium.
  • the monoclonal antibody 16G9mAb of Reference Example 1 (0.1, 2, 4, or 6 ⁇ g/mL/well) or the monoclonal antibody SSVmAb of Example 1 (4 ⁇ g/mL/well) was added at the start of mixed culture, and cultured for 3.5 days or longer under the conditions of 37°C, 5% CO 2 /95% air.
  • an immunosuppressive agent tacrolimus (FK506: Fujisawa Pharmaceutical Co., Ltd., 1 nM/well) was added as a positive control.
  • bromo deoxyuridine (BrdU) was added 15 hours before the end of culture. Then the proliferation potential of the cells treated with the immunosuppressive agent was measured using BrdU labeling & detection kit III (Roche Diagnostics K.K.) using the amount of BrdU incorporated into cellular DNA as an indicator.
  • Example 1 For Example 1 (SSVmAb), the absorbance which indicates the amount of incorporated BrdU was lower than that of Reference Example 1 (16G9mAb) and tacrolimus (FK506). In particular, when the absorbance 0.552 ⁇ 0.114 (mean ⁇ S.E.) of Example 1 (SSV mAb) and the absorbance 1.351 ⁇ 0.389 (mean ⁇ S.E.) of Reference Example 1 (16G9mAb) where the same amount was added (4 ⁇ g/mL/well) were compared, the mean of Example 1 was about 41% of that of Reference Example 1.
  • Test Example 4 Determination of the reactivity of the monoclonal antibody (SSVmAb) with T cells
  • spleen was removed from a C57BL/6 mouse (5 weeks old, female, CHARLES RIVER LABORATORIES JAPAN, INC.) to prepare whole splenic cells.
  • RPMI 1640 culture medium was also added to the residual insoluble spleen tissue again and allowed to stand, and then only the supernatant was collected, which was combined with the above-mentioned cell suspension to perform centrifugation at 1,500 rpm for 5 min.
  • 2 ml lysis buffer 150 mM NH 4 Cl/15 mM NaHCO 3 /0.1 mM EDTA-Na 2 , pH 7.3
  • 10 ml PBS was added. After washed 3 times by centrifugation at 1,500 rpm for 5 min, whole splenic cells were obtained.
  • the splenic cells were suspended at a ratio of 5x10 7 cells/200 ⁇ l in MACS buffer (0.5% bovine serum albumin (BSA, NACALAI TESQUE, INC., 08777-36)/PBS), to which 50 ⁇ l Biotin-antibody cocktail/5x10 7 cells was added and incubated at 4°C for 10 min. After this was suspended in 150 ⁇ l MACS buffer/5x10 7 cells, 100 ⁇ l anti-biotin micro beads/5x10 7 cells was added and incubated at 4°C for 15 min. To this, MACS buffer (10 ml) was added and washed by centrifugation at 1500 rpm for 5 min, and then the recovered cells were suspended in 500 ⁇ l MACS buffer.
  • MACS buffer (10 ml) was added and washed by centrifugation at 1500 rpm for 5 min, and then the recovered cells were suspended in 500 ⁇ l MACS buffer.
  • each sample was subjected to a FACSCalibur flow cytometer and CellQuest software (BD Bioscience) to analyze the number of 16G9 mAb or SSV mAb positive/CD3 positive T cells.
  • Example 1 (16G9 mAb) was compared with Example 1 (SSV mAb), no significant difference was observed for the reactivity with CD3 positive T cells, and these antibodies showed comparative reactivity (student t-test, p ⁇ 0.05).
  • Test Example 5 Identification of a target for down-regulation by SSV mAb
  • Example 1 Seven candidate proteins which may be down-regulated by Example 1 (SSV mAb) were identified by the proteome analysis.
  • ATP synthase was determined to be a target antigen of Example 1 (SSV mAb) by the method described below.
  • T cells from a Balb/c mouse having mitochondria ATP synthase knocked down were obtained using Accell siRNA kit from Thermo Fisher Scientific Inc.
  • Example 1 SSV mAb
  • Isotype IgG1 (eBioscience) was used as a control reagent.
  • T cells from a mouse not having the ATP synthase knocked down was used as a control test.
  • Example 1 significantly inhibited cell growth as compared with Isotype IgG1.
  • Fig. 6A and 6B suggests that the immunosuppressive activity of SSV mAb is decreased by knocking down the ATP synthase, and that SSV mAb down-regulates the activity of the ATP synthase upon immunosuppression.
  • Test Example 6 Identification of the sequence for the variable regions of the light and heavy chains of SSV mAb
  • Total RNA was prepared from the 1.6x10 7 cells of hybridoma obtained in Test Example 1 (Mouse-Mouse hybridoma SSV-C 93-3) using FastPure RNA Kit (TaKaRa).
  • TaKaRa FastPure RNA Kit
  • NIPPON GENE Poly (A) + Isolation Kit from Total RNA
  • 240 ⁇ g of total RNA was prepared from mRNA.
  • Ethanol precipitation was performed using Etachinmate (NIPPON GENE) to precipitate mRNA. After washed with 75% ethanol, mRNA was dried. To this, 10 ⁇ L RNase free water was added to dissolve mRNA.
  • the mRNA solution obtained was stored at -80°C.
  • SMARTer RACE cDNA Amplification Kit (Clontech)
  • cDNA for 5'-RACE was synthesized from 1 ⁇ g SSV hybridoma mRNA.
  • the cDNA solution obtained was stored at
  • CDR complementarity determining regions
  • a primer, 5'-CAC CAT GGA GTT AGT TTG GGC AGC AG-3' was produced.
  • a primer, 5'-CAC GAC TGA GGC ACC TCC AGA TG-3' was produced.
  • 5'-RACE was performed using cDNA as a template.
  • Advantage2 PCR Kit (Clontech) was used.
  • the reaction mixture was subjected to agarose electrophoresis, and a heavy chain 5'-RACE product of about 600 bp and a light chain 5'-RACE product of about 550 bp were purified from the gel using E.Z.N.A. Gel Extraction Kit (OMEGA bio-tek). This was linked to pGEM-T Easy Vector (Promega), with which Competent high E.coli DH5 ⁇ (TOYOBO) was transformed. From the resulting transformant, the plasmid was prepared using E.Z.N.A. Plasmid Miniprep KitI (OMEGA bio-tek). Using the prepared plasmid as a template, cyclical reactions were performed using BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems).
  • Position 1 to Position 66 of SEQ ID NO:5 corresponds to the base sequence of the light chain signal peptide
  • Position 1 to Position 57 of SEQ ID NO:10 corresponds to the base sequence of the heavy chain signal peptide.
  • the amino acid sequence of the light chain variable region was found to be represented by Position 23 to Position 128 of SEQ ID NO:6.
  • Position 1 to Position 22 of SEQ ID NO:6 corresponds to the amino acid sequence of the light chain signal peptide.
  • CDR1 is represented by RASSSVSYMH (SEQ ID NO:2)
  • CDR2 is represented by ATSNLAS (SEQ ID NO:3)
  • CDR3 is represented by QQWSSNPWT (SEQ ID NO:4).
  • amino acid sequence of the heavy chain variable region was found to be represented by Position 20 to Position 141 of SEQ ID NO:11.
  • Position 1 to Position 19 of SEQ ID NO:11 corresponds to the amino acid sequence of the heavy chain signal peptide.
  • CDR1 is represented by GYNMN (SEQ ID NO:7)
  • CDR2 is represented by NINPYYGSTSYNQKFKG (SEQ ID NO:8)
  • CDR3 is represented by SPYYSNYWRYFDY (SEQ ID NO:9).
  • LPS Lipopolysaccharide
  • SSV mAb dissolved in physiological saline was intraperitoneally administered totally 3 times, i.e., at 30 minutes before, 6 hours after and 12 hours after the intraperitoneal administration of LPS, in an amount of 100 ⁇ g/dose in terms of the amount of SSV mAb.
  • the survival of the animals thereafter was tested.
  • IgG (SIGMA) dissolved in physiological saline was administered in place of SSV mAb in the same manner.
  • the results are shown in Fig. 7 .
  • the survival rate at 70 hours after administration of LPS was 20% (cumulative survival rate: 0.2) in the control group (IgG) and 70% (cumulative survival rate: 0.7) in the SSV mAb-administered group.
  • the survival rate at 70 hours after administration of LPS (induction of sepsis) of the SSV mAb-administered group (SSV) was about 3.5 times of that of the control group, and was significantly higher than the control group (p ⁇ 0.05).
  • LPS lipopolysaccharide
  • SSV mAb dissolved in physiological saline was intraperitoneally administered totally 3 times, i.e., at 30 minutes before, 6 hours after and 12 hours after the intraperitoneal administration of LPS, in an amount of 100 ⁇ g/dose in terms of the amount of SSV mAb.
  • the survival of the animals thereafter was tested.
  • IgG (SIGMA) dissolved in physiological saline was administered in place of SSV mAb in the same manner.
  • the results are shown in Fig. 8 .
  • the survival rate at 24 hours after administration of LPS induction of sepsis was 20% in the control group (IgG) and 70% in the SSV mAb-administered group.
  • the survival rate at 70 hours after administration of LPS (induction of inflammation) of the SSV mAb-administered group (SSV) was about 3.5 times of that of the control group, and was significantly higher than the control group (p ⁇ 0.05).
  • Heart-derived blood or lung tissue was obtained from control group and SSV mAb-administered group under general anesthesia according to the method conducted by Hasegawa et al. (Surg Res. 2012 May 1;174(1):136-41 .).
  • the concentration of histone H1, histone H3 and H4 of the obtained samples were measured by using a commercially available measurement kit using ELISA.
  • Fig. 9A blood-derived serum
  • Fig. 9B lung tissue
  • the concentration of histone H1 in blood sample from the SSV mAb-administered group was almost kept constant without increase during the test.
  • the concentration of histone H1 in blood sample from the control group changes were observed during the test.
  • Fig. 10A blood-derived serum
  • Fig. 10B lung tissue
  • Fig. 11A blood-derived serum
  • Fig. 11B lung tissue
  • the concentrations of histone H3 in blood sample and inflammatory tissue (lung) from the SSV mAb-administered group were found to tend to be lower than the control group.
  • binding assays of SSV mAb with histone H1, histone H3 and histone H4 were carried out by ELISA in the same manner as Test Example 2.
  • SSV mAb was found to have a binding capacity with histone H1, histone H3 and histone H4 in vitro.
  • lung tissue sections were each obtained from rats of control group and SSV mAb-administered group, and stained by using hematoxylin and eosin stain (from Wako Pure Chemical Industries, Ltd.) according to the method conducted by Hasegawa et al. (Surg Res. 2012 May 1;174(1):136-41 .). Next, micrographs of the obtained samples were taken.
  • micrographs of lung tissue slices from healthy rats were taken in the same manner.
  • the scores of the SSV mAb-administered group was shown to be significantly lower than that of the control group.
  • test Example 8 serum was obtained from venous blood of the control group and the SSV mAb-administered group every 3 hours. Then, the concentrations of inflammatory cytokine (TNF- ⁇ , IL-1 ⁇ , IL-6) and inhibitory cytokine (IL-10) in obtained samples were measured by using a commercially available measurement kit using ELISA.
  • the values of inflammatory cytokine TNF- ⁇ , IL-1 ⁇ and IL-6 of the SSV mAb-administered group were significantly decreased compared to the control group.
  • the BUN and Cr values of the SSV mAb-administered group were significantly lower than that of the control group. Further, histological evaluation of kidney found that the state of the SSV mAb-administered group was better than that of the control group.
  • IgG IgG
  • BUN urea nitrogen
  • Cr creatinine
  • the BUN and Cr values of the SSV mAb-administered group were significantly lower than that of the control group. Further, histological evaluation of kidney found that the state of the SSV mAb-administered group was better than that of the control group.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Immunology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Zoology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Toxicology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
EP13751092.1A 2012-02-22 2013-02-22 Therapeutic agent for inflammatory disease Not-in-force EP2815763B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2012035965A JP2015117181A (ja) 2012-02-22 2012-02-22 敗血症治療剤
PCT/JP2013/054551 WO2013125687A1 (ja) 2012-02-22 2013-02-22 炎症疾患治療剤

Publications (3)

Publication Number Publication Date
EP2815763A1 EP2815763A1 (en) 2014-12-24
EP2815763A4 EP2815763A4 (en) 2015-07-22
EP2815763B1 true EP2815763B1 (en) 2018-06-13

Family

ID=49005863

Family Applications (1)

Application Number Title Priority Date Filing Date
EP13751092.1A Not-in-force EP2815763B1 (en) 2012-02-22 2013-02-22 Therapeutic agent for inflammatory disease

Country Status (8)

Country Link
US (2) US20150079090A1 (ja)
EP (1) EP2815763B1 (ja)
JP (1) JP2015117181A (ja)
KR (1) KR102159412B1 (ja)
CN (1) CN104379165B (ja)
IN (1) IN2014DN07875A (ja)
TW (1) TWI605059B (ja)
WO (1) WO2013125687A1 (ja)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9701739B2 (en) 2010-08-20 2017-07-11 Josai University Corporation Monoclonal antibody having immunosuppressive activity or antigen binding fragment thereof
CA3019560A1 (en) * 2016-03-29 2017-10-05 Obi Pharma, Inc. Antibodies, pharmaceutical compositions and methods
US10980894B2 (en) 2016-03-29 2021-04-20 Obi Pharma, Inc. Antibodies, pharmaceutical compositions and methods
EP3511419A4 (en) * 2016-09-23 2020-06-24 TFK Co., Ltd COMPOUND OR SALT THEREOF, ANTI-INFLAMMATORY AGENT, ANTI-CANCER AGENT FOR LUNG CANCER, METHOD FOR PRODUCING THE COMPOUND OR SALT THEREOF, METHOD FOR TREATING INFLAMMATORY DISEASE, AND METHOD FOR TREATING LUNG CANCER

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1820855A1 (en) * 2004-09-03 2007-08-22 Amateraspharma Inc. Anti-histone h1 monoclonal antibody and hybridoma capable of producing the same
EP2196212A1 (en) * 2007-10-04 2010-06-16 Josai University Corporation Preparation and method of administering vaccine and iontophoresis device using the preparation

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8716218B2 (en) * 2007-11-06 2014-05-06 Oklahoma Medical Research Foundation Extracellular histones as biomarkers for prognosis and molecular targets for therapy
US9701739B2 (en) * 2010-08-20 2017-07-11 Josai University Corporation Monoclonal antibody having immunosuppressive activity or antigen binding fragment thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1820855A1 (en) * 2004-09-03 2007-08-22 Amateraspharma Inc. Anti-histone h1 monoclonal antibody and hybridoma capable of producing the same
EP2196212A1 (en) * 2007-10-04 2010-06-16 Josai University Corporation Preparation and method of administering vaccine and iontophoresis device using the preparation

Also Published As

Publication number Publication date
CN104379165B (zh) 2018-08-03
KR102159412B1 (ko) 2020-09-23
EP2815763A4 (en) 2015-07-22
CN104379165A (zh) 2015-02-25
JP2015117181A (ja) 2015-06-25
US20150079090A1 (en) 2015-03-19
TW201350502A (zh) 2013-12-16
TWI605059B (zh) 2017-11-11
IN2014DN07875A (ja) 2015-04-24
WO2013125687A1 (ja) 2013-08-29
EP2815763A1 (en) 2014-12-24
US20170096478A1 (en) 2017-04-06
KR20140138699A (ko) 2014-12-04

Similar Documents

Publication Publication Date Title
CN108473566B (zh) 抗N3pGlu淀粉样蛋白β肽抗体及其用途
JP5893559B2 (ja) 新規な薬剤及びその使用
JP6967515B2 (ja) Ｐｄ−１抗体
RU2705255C2 (ru) Антитела против эотаксина 2, которые распознают дополнительные связывающие CCR3 хемокины
US20170096478A1 (en) Therapeutic agent for inflammatory disease
EP3556771B1 (en) Anti-claudin 5 antibody, and medicine containing said antibody
US20210403548A1 (en) Treating vascular disease and complications thereof
CN109384845B (zh) 一种cd40单克隆抗体、其制备方法及其应用
RU2559550C2 (ru) Моноклональное антитело, имеющее иммуносупрессивную активность, или его антигенсвязывающий фрагмент
DK2984108T3 (en) Anti-s100a7 antibodies for the treatment and diagnosis of cancer
EP4433509A1 (en) Methods to reverse treml1-induced immune suppression
JPWO2013125687A1 (ja) 炎症疾患治療剤
WO2024120484A1 (en) Antibodies against edil3 and methods of use thereof
WO2017133746A1 (en) Method for diagnosing and treating cancer using antibodies that bind to c1 inactivator, c reactive protein and/or complement component c4
村田憲治 Calcineurin inhibitors exacerbate coronary arteritis via the MyD88 signalling pathway in a murine model of Kawasaki disease
US20140050734A1 (en) Antibodies against the s100p protein for the treatment and diagnosis of cancer
CN118591554A (zh) 抗人cxcl1抗体
KR20230142834A (ko) 항-cd38 항체 및 이의 용도

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20140918

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAX Request for extension of the european patent (deleted)
RA4 Supplementary search report drawn up and despatched (corrected)

Effective date: 20150622

RIC1 Information provided on ipc code assigned before grant

Ipc: C07K 7/08 20060101ALI20150616BHEP

Ipc: A61P 13/12 20060101ALI20150616BHEP

Ipc: A61K 39/395 20060101AFI20150616BHEP

Ipc: A61P 31/04 20060101ALI20150616BHEP

Ipc: C07K 7/06 20060101ALI20150616BHEP

Ipc: C12N 15/09 20060101ALI20150616BHEP

Ipc: C07K 16/18 20060101ALI20150616BHEP

Ipc: A61P 29/00 20060101ALI20150616BHEP

Ipc: C12N 5/10 20060101ALI20150616BHEP

Ipc: C07K 16/44 20060101ALI20150616BHEP

Ipc: A61K 39/00 20060101ALI20150616BHEP

17Q First examination report despatched

Effective date: 20160614

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20180104

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1007789

Country of ref document: AT

Kind code of ref document: T

Effective date: 20180615

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602013038906

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20180613

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180913

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180913

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180914

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1007789

Country of ref document: AT

Kind code of ref document: T

Effective date: 20180613

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181013

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602013038906

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20190314

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190222

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190228

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190228

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190222

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181015

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190222

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20130222

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20220223

Year of fee payment: 10

Ref country code: DE

Payment date: 20220217

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20220218

Year of fee payment: 10

Ref country code: FR

Payment date: 20220216

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180613

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602013038906

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20230222

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230222

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230222

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230222

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230228

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230901